| Weight | 337.456 g/mol |
|---|---|
| Formula | C8H15N7O2S3 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
76824-35-6 (76824-35-6)
Famotidine · Pepcid · MK 208
Score:
#1502 in Biology
,
#1763 in Chemistry
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- Famotidine for the prevention of gastric and duodenal ulcers caused by nonsteroidal antiinflammatory drugs (The New England Journal of Medicine, 1996)
- Famotidine for the prevention of peptic ulcers and oesophagitis in patients taking low-dose aspirin (FAMOUS): a phase III, randomised, double-blind, placebo-controlled trial (The Lancet, 2009)
- Famotidine: an updated review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in peptic ulcer disease and other allied diseases (Drugs, 1989)
- Famotidine, a New, Potent, Long-Acting Histamine H2-Receptor Antagonist: Comparison With Cimetidine and Ranitidine in the Treatment of Zollinger-Ellison Syndrome (Gastroenterology, 1985)
- A study of carboxylic-modified mesoporous silica in controlled delivery for drug famotidine (Journal of Solid State Chemistry, 2006)
- Famotidine for healing and maintenance in nonsteroidal anti- inflammatory drug-associated gastroduodenal ulceration (Gastroenterology, 1997)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Famotidine
- Pepcid
- MK 208
- Famotidine Hydrochloride
- YM11170
- YM-11170
- YM 11170
- MK-208
- MK208
-
SMILESC1=C(N=C(S1)N=C(N)N)CSCCC(=NS(=O)(=O)N)N
-
InChIKeyXUFQPHANEAPEMJ-UHFFFAOYSA-N
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